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Efficacy and Safety of Switching to Teneligliptin in Patients with Type 2 Diabetes Inadequately Controlled with Dipeptidyl Peptidase-4 Inhibitors: A 12-Week Interim Report

INTRODUCTION: Teneligliptin, an antidiabetic agent classified as a class III dipeptidyl peptidase-4 (DPP-4) inhibitor, has a unique structural feature that provides strong binding to DPP-4 enzymes. We investigated the efficacy and safety of switching patients with type 2 diabetes mellitus (T2DM) who...

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Autores principales: Kim, Hae Jin, Kim, Young Sik, Lee, Chang Beom, Choi, Moon-Gi, Chang, Hyuk-Jae, Kim, Soo Kyoung, Yu, Jae Myung, Kim, Tae Ho, Lee, Ji Hyun, Ahn, Kyu Jeung, Kim, Kyoungmin, Lee, Kwan Woo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6612358/
https://www.ncbi.nlm.nih.gov/pubmed/31079357
http://dx.doi.org/10.1007/s13300-019-0628-0
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author Kim, Hae Jin
Kim, Young Sik
Lee, Chang Beom
Choi, Moon-Gi
Chang, Hyuk-Jae
Kim, Soo Kyoung
Yu, Jae Myung
Kim, Tae Ho
Lee, Ji Hyun
Ahn, Kyu Jeung
Kim, Kyoungmin
Lee, Kwan Woo
author_facet Kim, Hae Jin
Kim, Young Sik
Lee, Chang Beom
Choi, Moon-Gi
Chang, Hyuk-Jae
Kim, Soo Kyoung
Yu, Jae Myung
Kim, Tae Ho
Lee, Ji Hyun
Ahn, Kyu Jeung
Kim, Kyoungmin
Lee, Kwan Woo
author_sort Kim, Hae Jin
collection PubMed
description INTRODUCTION: Teneligliptin, an antidiabetic agent classified as a class III dipeptidyl peptidase-4 (DPP-4) inhibitor, has a unique structural feature that provides strong binding to DPP-4 enzymes. We investigated the efficacy and safety of switching patients with type 2 diabetes mellitus (T2DM) who had inadequate glycemic control on a stable dose of other DPP-4 inhibitors to teneligliptin. METHODS: Patients with T2DM whose glycosylated hemoglobin (HbA1c) levels were ≥ 7% despite taking DPP-4 inhibitors other than teneligliptin, with or without other hypoglycemic agents, for at least 3 months were enrolled. The DPP-4 inhibitors taken before participating in the study were switched to 20 mg qd teneligliptin, and this was to be maintained for 52 weeks. The primary end point was the change in HbA1c levels after 12 weeks. Metabolic parameters including fasting plasma glucose (FPG) and blood lipids were assessed also. To assess safety, adverse and hypoglycemic events were monitored. The data from baseline to week 12 were used for analysis in this interim report. RESULTS: The mean change in HbA1c levels from baseline to week 12 was − 0.44%. At week 12, the percentage of patients achieving HbA1c < 7.0% was 31.6% and that of achieving HbA1c < 6.5% was 11.4%, respectively. In 41.2% of patients, the HbA1c levels decreased by at least 0.5% at 12 weeks. The mean change in FPG levels from baseline to week 12 was − 11.5 mg/dl. No severe hypoglycemia was reported. CONCLUSION: After switching to teneligliptin, HbA1c levels decreased significantly in patients with T2DM inadequately controlled with other DPP-4 inhibitors. TRIAL REGISTRATION: ClinicalTrials.gov, NCT03793023. FUNDING: Handok Inc. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s13300-019-0628-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-66123582019-07-23 Efficacy and Safety of Switching to Teneligliptin in Patients with Type 2 Diabetes Inadequately Controlled with Dipeptidyl Peptidase-4 Inhibitors: A 12-Week Interim Report Kim, Hae Jin Kim, Young Sik Lee, Chang Beom Choi, Moon-Gi Chang, Hyuk-Jae Kim, Soo Kyoung Yu, Jae Myung Kim, Tae Ho Lee, Ji Hyun Ahn, Kyu Jeung Kim, Kyoungmin Lee, Kwan Woo Diabetes Ther Original Research INTRODUCTION: Teneligliptin, an antidiabetic agent classified as a class III dipeptidyl peptidase-4 (DPP-4) inhibitor, has a unique structural feature that provides strong binding to DPP-4 enzymes. We investigated the efficacy and safety of switching patients with type 2 diabetes mellitus (T2DM) who had inadequate glycemic control on a stable dose of other DPP-4 inhibitors to teneligliptin. METHODS: Patients with T2DM whose glycosylated hemoglobin (HbA1c) levels were ≥ 7% despite taking DPP-4 inhibitors other than teneligliptin, with or without other hypoglycemic agents, for at least 3 months were enrolled. The DPP-4 inhibitors taken before participating in the study were switched to 20 mg qd teneligliptin, and this was to be maintained for 52 weeks. The primary end point was the change in HbA1c levels after 12 weeks. Metabolic parameters including fasting plasma glucose (FPG) and blood lipids were assessed also. To assess safety, adverse and hypoglycemic events were monitored. The data from baseline to week 12 were used for analysis in this interim report. RESULTS: The mean change in HbA1c levels from baseline to week 12 was − 0.44%. At week 12, the percentage of patients achieving HbA1c < 7.0% was 31.6% and that of achieving HbA1c < 6.5% was 11.4%, respectively. In 41.2% of patients, the HbA1c levels decreased by at least 0.5% at 12 weeks. The mean change in FPG levels from baseline to week 12 was − 11.5 mg/dl. No severe hypoglycemia was reported. CONCLUSION: After switching to teneligliptin, HbA1c levels decreased significantly in patients with T2DM inadequately controlled with other DPP-4 inhibitors. TRIAL REGISTRATION: ClinicalTrials.gov, NCT03793023. FUNDING: Handok Inc. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s13300-019-0628-0) contains supplementary material, which is available to authorized users. Springer Healthcare 2019-05-11 2019-08 /pmc/articles/PMC6612358/ /pubmed/31079357 http://dx.doi.org/10.1007/s13300-019-0628-0 Text en © The Author(s) 2019 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research
Kim, Hae Jin
Kim, Young Sik
Lee, Chang Beom
Choi, Moon-Gi
Chang, Hyuk-Jae
Kim, Soo Kyoung
Yu, Jae Myung
Kim, Tae Ho
Lee, Ji Hyun
Ahn, Kyu Jeung
Kim, Kyoungmin
Lee, Kwan Woo
Efficacy and Safety of Switching to Teneligliptin in Patients with Type 2 Diabetes Inadequately Controlled with Dipeptidyl Peptidase-4 Inhibitors: A 12-Week Interim Report
title Efficacy and Safety of Switching to Teneligliptin in Patients with Type 2 Diabetes Inadequately Controlled with Dipeptidyl Peptidase-4 Inhibitors: A 12-Week Interim Report
title_full Efficacy and Safety of Switching to Teneligliptin in Patients with Type 2 Diabetes Inadequately Controlled with Dipeptidyl Peptidase-4 Inhibitors: A 12-Week Interim Report
title_fullStr Efficacy and Safety of Switching to Teneligliptin in Patients with Type 2 Diabetes Inadequately Controlled with Dipeptidyl Peptidase-4 Inhibitors: A 12-Week Interim Report
title_full_unstemmed Efficacy and Safety of Switching to Teneligliptin in Patients with Type 2 Diabetes Inadequately Controlled with Dipeptidyl Peptidase-4 Inhibitors: A 12-Week Interim Report
title_short Efficacy and Safety of Switching to Teneligliptin in Patients with Type 2 Diabetes Inadequately Controlled with Dipeptidyl Peptidase-4 Inhibitors: A 12-Week Interim Report
title_sort efficacy and safety of switching to teneligliptin in patients with type 2 diabetes inadequately controlled with dipeptidyl peptidase-4 inhibitors: a 12-week interim report
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6612358/
https://www.ncbi.nlm.nih.gov/pubmed/31079357
http://dx.doi.org/10.1007/s13300-019-0628-0
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